Canonical Allele Identifier: CA2620119500

Gene: KITLG

Linked Data

• gnomAD v4: 12-88532355-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88532355T>C , CM000674.2:g.88532355T>C	GRCh38
NC_000012.11:g.88926132T>C , CM000674.1:g.88926132T>C	GRCh37
NC_000012.10:g.87450263T>C	NCBI36
NG_012098.1:g.53107A>G
NG_012098.2:g.53107A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347404.10:c.192+86A>G	ENSP00000054216.5:n.192+86A>G
ENST00000644744.1:c.192+86A>G MANE Select	ENSP00000495951.1:n.192+86A>G
ENST00000646633.1:c.*193+86A>G	ENSP00000494139.1:n.*193+86A>G
ENST00000228280.9:c.192+86A>G	ENSP00000228280.5:n.192+86A>G
ENST00000347404.9:c.192+86A>G	ENSP00000054216.5:n.192+86A>G
ENST00000357116.4:c.-47-25218A>G	ENSP00000474021.1:n.-47-25218A>G
ENST00000378535.4:n.135+86A>G
ENST00000552044.1:c.39+86A>G	ENSP00000475042.1:n.39+86A>G
NM_000899.4:c.192+86A>G	NP_000890.1:n.192+86A>G
NM_003994.5:c.192+86A>G	NP_003985.2:n.192+86A>G
NM_000899.5:c.192+86A>G MANE Select	NP_000890.1:n.192+86A>G
NM_003994.6:c.192+86A>G	NP_003985.2:n.192+86A>G